% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@INBOOK{Ermer:162762,
author = {Ermer, Veronika and Nicotera, Pierluigi and Stainbrook,
Sarah C.},
title = {{C}ell {D}eath | {C}ell {D}eath by {A}poptosis and
{N}ecrosis},
volume = {5},
publisher = {Elsevier},
reportid = {DZNE-2021-01418},
pages = {38-41},
year = {2021},
comment = {Encyclopedia of Biological Chemistry III / Ermer, Veronika
; : Elsevier, 2021, ; ISBN: 9780128220405 ;
doi:10.1016/B978-0-12-819460-7.00270-X},
booktitle = {Encyclopedia of Biological Chemistry
III / Ermer, Veronika ; : Elsevier,
2021, ; ISBN: 9780128220405 ;
doi:10.1016/B978-0-12-819460-7.00270-X},
abstract = {Various genetically encoded programs involved in the
signaling, initiation, and execution of cell death decide
cells׳ fate during development and adult life. These
programs can execute physiological cell death during
development or tissue turnover, and are also involved in the
inappropriate elimination of cells under pathological
conditions. Because balanced cell turnover is essential for
life, defects in cell elimination can also result in
disease, the foremost example being cancer. In many
circumstances, both physiological cell death and cell death
in pathological settings have similar morphological and
biochemical characteristics. Perhaps the best-characterized
biochemical and morphological changes during a cell death
program are those defined as apoptosis. Apoptosis is
characterized by condensation and fragmentation of the
nucleus with shrinkage of the cytoplasm and exposure of
surface molecules that facilitate recognition of the dying
cells by phagocytes. However, other types of cell death are
present and are strictly regulated in vivo, including cell
lysis/necrosis or autophagy. Imbalance in cellular calcium
regulation has been involved in both apoptotic and
nonapoptotic cell death. Calcium can be a signal for cell
death or simply a downstream consequence of the activation
of the death machinery.},
cin = {AG Nicotera / Scientific board / AG Bano},
cid = {I:(DE-2719)5000018 / I:(DE-2719)1030000 /
I:(DE-2719)1013003},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)7},
doi = {10.1016/B978-0-12-819460-7.00270-X},
url = {https://pub.dzne.de/record/162762},
}